PT-141 (Bremelanotide)
Typical dose
0.5–2 mg
~45 min before, as needed · SubQ
Half-life
2-3 hours
What is PT-141 (Bremelanotide)?
Melanocortin receptor agonist originally developed for sexual dysfunction. Acts centrally on the brain, not vascularly like PDE5 inhibitors.
How PT-141 (Bremelanotide) works
Agonizes MC3R and MC4R in the brain, stimulating sexual arousal pathways.
Benefits & uses
- Libido enhancement
- Sexual arousal
- Works in both men and women
Common uses: Sexual desire, arousal, erectile function in both sexes.
PT-141 (Bremelanotide) dosage
- Typical dose
- Typical: 0.5–2 mg SubQ, ~45 min before activity, as needed (not daily).
- Protocol notes
- 1-2mg SubQ as needed. Max 1 dose per 24h.
PT-141 (Bremelanotide) half-life
2-3 hours
PT-141 (Bremelanotide) side effects
Nausea (common), facial flushing, transient BP increase, headache.
- Nausea (common)
- Facial flushing
- Transient BP increase
- Headache
Warnings & monitoring
- Research use only outside FDA indication
- Nausea common
- Transient blood pressure increase
- Not for cardiovascular disease patients
Preparation & storage
- Preparation
- Mix a 10 mg vial with 2 mL bac water → 5 mg/mL. A 1 mg dose = 0.2 mL = 20 units.
- Reconstitution
- Reconstitute a 10 mg vial with 2 mL BAC water → 5 mg/mL. A 1 mg dose = 0.2 mL = 20 units on a U-100 syringe.
- Storage
- Refrigerate pens or vials per manufacturer. Protect from light.
PT-141 (Bremelanotide) interactions
with Melanotan II
Caution · moderateBoth target melanocortin receptors. Stacking amplifies nausea, flushing, and prolonged erections (priapism risk in men).
Timing: Separate by at least 24 hours; do not co-administer
with Melanotan II
Caution · moderatePT-141 (Bremelanotide) is derived directly from Melanotan II. Using both simultaneously gives no additional benefit and significantly increases nausea, flushing, spontaneous erections, and blood pressure elevation.
Timing: Do not use both; choose one. PT-141 is derived from Melanotan II.
with Tadalafil
Caution · mildBoth compounds lower blood pressure via different mechanisms (MC4R vs PDE5). Combined use can cause significant hypotension — start with minimal doses and assess tolerance individually before combining.
Timing: Use lowest effective doses; monitor blood pressure; do not combine with alcohol
with BPC-157
CompatibleBPC-157 (healing/gut repair) and PT-141 (sexual function/MC4R agonist) act on entirely different receptor systems with no known pharmacological interaction.
Timing: Independent injection timing; no pharmacological conflict
with BPC-157
CompatibleNo known interaction. PT-141 (Bremelanotide) activates melanocortin receptors for sexual arousal; BPC-157 for systemic healing and inflammation. Complementary use in optimization protocols.
Timing: Administer separately; PT-141 subcutaneous 1–2h before, BPC-157 as scheduled
